FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TA VBR

DI: M682215672200 · Model: 2156-7220 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TA VBR
Primary DI
M682215672200
Version / Model
2156-7220
Catalog Number
2156-7220
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
6
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
5d5ffd01-6669-49fa-9260-58fbe802fbef
Distribution End Date
2020-09-21

Device Description

7 DEG LORDOTIC, RASP, LARGE, 20MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary M682215672200

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Lordotic Angle 7 Deg
Height 20 Millimeter
Depth 24 Millimeter
Angle 7 degree
Device Size Text, specify width(MLxAP), 36 x 24, mm
Width 36 Millimeter